3-(3-{[5-(2-adamantan-1-ylethyl)-2-o-tolyl-1H-imidazole-4-carbonyl]amino}phenyl)propionic acid tert-butyl ester

Base Information

Chemical Name:3-(3-{[5-(2-adamantan-1-ylethyl)-2-o-tolyl-1H-imidazole-4-carbonyl]amino}phenyl)propionic acid tert-butyl ester
CAS No.:269071-09-2
Molecular Formula:C₃₆H₄₅N₃O₃
Molecular Weight:567.772
Hs Code.:

Synonyms:3-(3-{[5-(2-adamantan-1-ylethyl)-2-o-tolyl-1H-imidazole-4-carbonyl]amino}phenyl)propionic acid tert-butyl ester

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Chemical Property of 3-(3-{[5-(2-adamantan-1-ylethyl)-2-o-tolyl-1H-imidazole-4-carbonyl]amino}phenyl)propionic acid tert-butyl ester

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Technology Process of 3-(3-{[5-(2-adamantan-1-ylethyl)-2-o-tolyl-1H-imidazole-4-carbonyl]amino}phenyl)propionic acid tert-butyl ester

There total 4 articles about 3-(3-{[5-(2-adamantan-1-ylethyl)-2-o-tolyl-1H-imidazole-4-carbonyl]amino}phenyl)propionic acid tert-butyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 269071-75-2
5-adamantan-1-yl-2,3-dioxopentanoic acid ethyl ester

: 269071-09-2
3-(3-{[5-(2-adamantan-1-ylethyl)-2-o-tolyl-1H-imidazole-4-carbonyl]amino}phenyl)propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 56 percent / NH₄OAc; AcOH / 2 h / 70 °C

2: 80 percent / aq. NaOH / ethanol / 24 h / Heating

3: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 4-(dimethylamino)pyridine; 1-hydroxybenzotriazole / dimethylformamide / 20 °C

With dmap; sodium hydroxide; ammonium acetate; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm0490686

Reference yield:

: 269071-81-0
5-(2-adamantan-1-ylethyl)-2-o-tolyl-1H-imidazole-4-carboxylic acid ethyl ester

: 269071-09-2
3-(3-{[5-(2-adamantan-1-ylethyl)-2-o-tolyl-1H-imidazole-4-carbonyl]amino}phenyl)propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / aq. NaOH / ethanol / 24 h / Heating

2: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 4-(dimethylamino)pyridine; 1-hydroxybenzotriazole / dimethylformamide / 20 °C

With dmap; sodium hydroxide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm0490686

Reference yield:

: 455333-76-3
5-adamantan-1-yl-3-oxo-2-(triphenyl-λ⁵-phosphanylidene)pentanoic acid ethyl ester

: 269071-09-2
3-(3-{[5-(2-adamantan-1-ylethyl)-2-o-tolyl-1H-imidazole-4-carbonyl]amino}phenyl)propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 70 percent / OXONE / tetrahydrofuran / 16 h / 20 °C

2: 56 percent / NH₄OAc; AcOH / 2 h / 70 °C

3: 80 percent / aq. NaOH / ethanol / 24 h / Heating

4: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 4-(dimethylamino)pyridine; 1-hydroxybenzotriazole / dimethylformamide / 20 °C

With dmap; Oxone; sodium hydroxide; ammonium acetate; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm0490686